IP Library Granted Patent US 10,758,550
Granted Patent B2
US 10,758,550 · App. 15/903,597 · Granted Sep 1, 2020

Treatment of allergic rhinitis using a combination of mometasone and olopatadine

Inventors: Neelima Khairatkar-Joshi (Thane, IN); Abhay Kulkarni (Navi Mumbai, IN); Pradeep D. Wale (Maharashtra, IN); Vikram M. Bhosale (Mumbai, IN); Piyush Agarwal (Mumbai, IN); Patrick Keohane (London, GB); Sudeesh K. Tantry (Jamison, PA); Chad Oh (San Francisco, CA)
Assignee: GLENMARK SPECIALTY S.A.
A61K31/58A61K9/0043A61K31/335A61K31/573A61P11/02A61P27/14A61P37/08A61M11/007A61M15/08
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Quick Facts
Patent No.
US 10,758,550
App. No.
15/903,597
Granted
Sep 1, 2020
Kind
B2
Abstract

The present invention relates to a method of treating allergic rhinitis in a subject (e.g., a pediatric human subject) in need thereof comprising nasally administering to the subject an effective amount of a fixed-dose pharmaceutical composition comprising mometasone or its salt and olopatadine or its salt.

Claims (32)

1. A method of providing a faster onset of action for relief of allergic rhinitis in a pediatric human subject in need thereof, the method comprising nasally administering to a subject twice daily, one spray per nostril of a fixed-dose pharmaceutical composition comprising mometasone furoate and olopatadine hydrochloride, wherein (i) each spray comprises about 25 mcg of mometasone furoate and about 665 mcg olopatadine hydrochloride, and (ii) the administration provides relief from one or more symptoms of allergic rhinitis faster than nasal administration of 25 mcg mometasone furoate or 665 mcg olopatadine hydrochloride per nostril alone.

2. The method of claim 1 , wherein the one or more symptoms are selected from nasal symptoms.

3. The method of claim 2 , wherein the nasal symptoms are selected from nasal congestion, rhinorrhea, itching and sneezing.

4. The method of claim 1 , wherein the human subject is 2 to under 12 years of age.

5. The method of claim 1 , wherein the human subject is 2 to under 6 years of age.

6. The method of claim 1 , wherein the human subject is 6 to under 12 years of age.

7. The method of claim 1 , wherein the allergic rhinitis is selected from seasonal allergic rhinitis, perennial allergic rhinitis, and persistent allergic rhinitis.

8. The method of claim 7 , wherein the allergic rhinitis is seasonal allergic rhinitis.

9. The method of claim 7 , wherein the allergic rhinitis is perennial allergic rhinitis.

10. The method of claim 1 , wherein the pediatric human subject is 2 years of age or older.

11. A method of treating one or more symptoms associated with allergic rhinitis in a pediatric human subject in need thereof comprising nasally administering twice daily, one spray per nostril of a fixed-dose pharmaceutical composition comprising mometasone furoate and olopatadine hydrochloride, wherein (i) each spray comprises about 25 mcg of mometasone furoate and about 665 mcg olopatadine hydrochloride and (ii) the administration of the pharmaceutical composition provides relief from one or more symptoms of allergic rhinitis within 15 minutes of administration.

12. A method of treating one or more symptoms associated with allergic rhinitis in a pediatric human subject in need thereof comprising nasally administering twice daily, one spray per nostril of a fixed-dose pharmaceutical composition comprising mometasone furoate and olopatadine hydrochloride, wherein (i) each spray comprises about 25 mcg of mometasone furoate and about 665 mcg olopatadine hydrochloride and (ii) the administration of the pharmaceutical composition provides relief from one or more symptoms of allergic rhinitis within 10 minutes of administration.

13. The method of claim 10 , wherein the one or more symptoms are selected from nasal symptoms.

14. The method of claim 13 , wherein the nasal symptoms are selected from nasal congestion, rhinorrhea, itching and sneezing.

15. The method of claim 10 , wherein the human subject is at 2 to under 12 years of age.

16. The method of claim 10 , wherein the human subject is 6 to under 12 years of age.

17. The method of claim 10 , wherein the human subject is 2 to under 6 years of age.

18. The method of claim 10 , wherein the allergic rhinitis is selected from seasonal allergic rhinitis, perennial allergic rhinitis, and persistent allergic rhinitis.

19. The method of claim 18 , wherein the allergic rhinitis is seasonal allergic rhinitis.

20. The method of claim 18 , wherein the allergic rhinitis is perennial allergic rhinitis.

21. The method of claim 10 , wherein the allergic rhinitis is seasonal allergic rhinitis.

22. The method of claim 10 , wherein the allergic rhinitis is perennial allergic rhinitis.

23. A method of treating one or more symptoms associated with allergic rhinitis in a pediatric human subject in need thereof comprising twice daily nasal administration of a single dose of a pharmaceutical composition comprising mometasone furoate and olopatadine hydrochloride, wherein (i) a single dose of the composition provides about 1330 mcg olopatadine hydrochloride and about 50 mcg mometasone furoate and (ii) the administration of the pharmaceutical composition provides relief from one or more symptoms of allergic rhinitis within 15 minutes of administration.

24. A method of treating one or more symptoms associated with allergic rhinitis in a pediatric human subject in need thereof comprising twice daily nasal administration of a single dose of a pharmaceutical composition comprising mometasone furoate and olopatadine hydrochloride, wherein (i) a single dose of the composition provides about 1330 mcg olopatadine hydrochloride and about 50 mcg mometasone furoate and (ii) the administration of the pharmaceutical composition provides relief from one or more symptoms of allergic rhinitis within 10 minutes of administration.

25. A method of providing a faster onset of action for relief of allergic rhinitis in a pediatric human subject in need thereof, the method comprising twice daily nasal administration of a single dose of a pharmaceutical composition comprising mometasone furoate and olopatadine hydrochloride, wherein (i) a single dose of the composition provides about 1330 mcg olopatadine hydrochloride and about 50 mcg mometasone furoate, and (ii) the administration provides relief from one or more symptoms of allergic rhinitis faster than nasal administration of 50 mcg mometasone furoate or 1330 mcg olopatadine hydrochloride alone.

26. The method of claim 25 , wherein the pediatric human subject is 2 years of age or older.

27. The method of claim 25 , wherein the human subject is 2 to under 12 years of age.

28. The method of claim 25 , wherein the human subject is 2 to under 6 years of age.

29. The method of claim 25 , wherein the human subject is 6 to under 12 years of age.

30. The method of claim 26 , wherein the one or more symptoms are selected from nasal symptoms.

31. The method of claim 26 , wherein the allergic rhinitis is seasonal allergic rhinitis.

32. The method of claim 26 , wherein the allergic rhinitis is perennial allergic rhinitis.

Assignments (2)
CHANGE OF ADDRESS Recorded Oct 26, 2023
From: GLENMARK SPECIALTY S.A.
To: GLENMARK SPECIALTY S.A.
Reel/Frame 065379/0694 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2018
From: KHAIRATKAR-JOSHI, NEELIMA; KULKARNI, ABHAY; WALE, DINESH PRADEEP; BHOSALE, VIKRAM MANSINGH; AGARWAL, PIYUSH; KEOHANE, PATRICK; TANTRY, SUDEESH K; OH, CHAD
To: GLENMARK SPECIALTY S.A.
Reel/Frame 045697/0854 →
Priority Claims (1)
IN 3174/MUM/2013 · Oct 4, 2013 · national
Continuity (7)
Continuation In Part 15842063 · Dec 14, 2017
Continuation In Part 15716661 · Sep 27, 2017
Continuation In Part 15691500 · Aug 30, 2017
Continuation In Part 15636120 · Jun 28, 2017
Continuation In Part 14682001 · Apr 8, 2015
Continuation In Part 14506122 · Oct 3, 2014
Related Publication 20190030047A1 · Jan 31, 2019